Laboratory of Reproductive Biology, Graduate School of Agricultural Science, Kobe University, Kobe, Japan.
Laboratory of Reproductive Biology, Graduate School of Agricultural Science, Kobe University, Kobe, Japan.
Theriogenology. 2014 May;81(8):1012-1020.e1. doi: 10.1016/j.theriogenology.2014.01.014. Epub 2014 Jan 31.
The characterization and quantitative analyses of the key transcription factors for spermiogenesis are necessary in the identification of causal factors for the production of the seemingly normal sperm with dysfunctions in Japanese Black bulls and further elucidation of whole aspect of molecular mechanisms for spermiogenesis in livestock. The objective of this study was to obtain the information regarding the characterization and individual changes of an activator cAMP-responsive element modulator (CREM), which is necessary to the normal progress of spermiogenesis and is required for the transcriptional activity of genes coding essential factors for the sperm fertilization ability in rodents, using testes from 21 Japanese Black bulls with the ability to produce sperm indicating the normal motility and morphology. The bull CREM ταγ (one of activator variants) was detected in testes more strongly than livers by reverse transcription-polymerase chain reaction and Northern blotting. This variant was localized in the nuclei of spermatids as shown by indirect immunofluorescence with the homemade mouse antiserum. The motility and morphology of the cauda epididymal sperm from 16 Japanese Black bulls were examined before the quantitative analyses of testicular activator CREM to confirm the ability to produce sperm with normal motility and morphology in these males. The percentages of the motile sperm, those of the sperm with the normal acrosomes, and those of morphologically normal sperm were 60.0% to 90.0%, 88.0% to 100%, and 83.0% to 97.9%, respectively. The quantitative analyses with real-time polymerase chain reaction using the testicular RNA from the same bulls revealed that the relative expression levels of activator CREM variants in testes varied significantly among these bulls in the range from 0.56 to 1.64 (P < 0.05). These results are consistent with the suggestions that CREM ταγ are involved in the spermiogenesis in the testes of Japanese Black bulls and that the expression levels of the activator CREM variant mRNAs in the testes are varied significantly among individual bulls that have the ability to produce sperm with the normal motility and morphology.
在鉴定日本黑牛产生看似正常但功能障碍精子的因果因素以及进一步阐明家畜精子发生的整体分子机制方面,对精子发生的关键转录因子进行特征描述和定量分析是必要的。本研究的目的是获得关于 cAMP 反应元件调节剂(CREM)激活剂的特征描述和个体变化的信息,该调节剂对于精子发生的正常进展是必要的,并且对于编码啮齿动物精子受精能力所必需的基因的转录活性也是必需的。在所研究的 21 头具有产生正常活力和形态精子能力的日本黑公牛的睾丸中使用了这种信息。通过逆转录-聚合酶链反应和 Northern 印迹法,在睾丸中比在肝脏中检测到更强的公牛 CREM ταγ(一种激活变体)。通过使用自制的小鼠抗血清进行间接免疫荧光,该变体定位于精母细胞的核内。在对睾丸激活 CREM 进行定量分析之前,检查了 16 头日本黑公牛的附睾尾部精子的活力和形态,以确认这些雄性具有产生具有正常活力和形态的精子的能力。运动精子的百分比、具有正常顶体的精子的百分比和形态正常的精子的百分比分别为 60.0%至 90.0%、88.0%至 100%和 83.0%至 97.9%。使用来自同一公牛睾丸的 RNA 进行实时聚合酶链反应的定量分析显示,在这些公牛中,激活 CREM 变体的相对表达水平在 0.56 到 1.64 之间变化显著(P<0.05)。这些结果与 CREM ταγ 参与日本黑公牛睾丸精子发生的建议以及具有产生具有正常活力和形态的精子的能力的个体公牛睾丸中激活 CREM 变体 mRNA 的表达水平变化显著的建议一致。